Variant #0000404882 (NC_000005.9:g.36971127C>G, NM_133433.3:c.760C>G (NIPBL))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.36971127C>G
DNA change (hg38) g.36971025C>G
Published as -
ISCN -
DB-ID NIPBL_000233 See all 2 reported entries
Variant remarks yeast two-hybrid analysis: no effect on NIBPL-MAU2 interaction
Reference ESHG2010 Braunholz P11.015
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jorge Oliveira
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Jorge Oliveira
Date created 2010-06-14 22:35:13 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NIPBL NM_133433.3 -?/. 7 c.760C>G r.(?) p.Leu254Val


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